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JAY FEINGOLD, MD, PHD
MD, PHD
Pediatrics Physician
NPI: 1639512841Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
MD071474L(PA)
Research & Publications (20)
Long-term outcome of presymptomatic testing in Huntington disease.
PMID 18716614·Eur J Hum Genet·2009
8-other
Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients.
PMID 19092771·Eur J Hum Genet·2009
8-other
Effect of temsirolimus versus interferon-alpha on outcome of patients with advanced renal cell carcinoma of different tumor histologies.
PMID 19229667·Med Oncol·2009
3-trial
Analysis of PTEN and HIF-1alpha and correlation with efficacy in patients with advanced renal cell carcinoma treated with temsirolimus versus interferon-alpha.
PMID 19526589·Cancer·2009
3-trial
The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonism.
PMID 18785640·Mov Disord·2008
8-other
Identifying modifier genes of monogenic disease: strategies and difficulties.
PMID 18784943·Hum Genet·2008
6-review
Temsirolimus safety profile and management of toxic effects in patients with advanced renal cell carcinoma and poor prognostic features.
PMID 18385198·Ann Oncol·2008
2-rct
Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosis.
PMID 19009622·Pediatr Pulmonol·2008
8-other
Revisiting metatropic dysplasia: presentation of a series of 19 novel patients and review of the literature.
PMID 18348257·Am J Med Genet A·2008
6-review
Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse).
PMID 18407552·Hum Mutat·2008
5-case
Population history and infrequent mutations: how old is a rare mutation? GUCY2D as a worked example.
PMID 17684531·Eur J Hum Genet·2008
8-other
Early energy deficit in Huntington disease: identification of a plasma biomarker traceable during disease progression.
PMID 17653274·PLoS One·2007
8-other
Glucocorticoid receptor gene polymorphisms associated with progression of lung disease in young patients with cystic fibrosis.
PMID 18047640·Respir Res·2007
4-observational
ReFacto and Advate: a single-dose, randomized, two-period crossover pharmacokinetics study in subjects with haemophilia A.
PMID 17286764·Haemophilia·2007
4-observational
Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung disease.
PMID 17397038·Hum Mutat·2007
8-other
Disease-associated variants of the rod-derived cone viability factor (RdCVF) in Leber congenital amaurosis. Rod-derived cone viability variants in LCA.
PMID 17249548·Adv Exp Med Biol·2006
7-preclinical
[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas].
PMID 16677780·Pathol Biol (Paris)·2006
6-review
Female predominance and transmission distortion in the long-QT syndrome.
PMID 17192539·N Engl J Med·2006
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2 HILTON CT
PARSIPPANY, NJ 07054 - Phone
- (973) 944-2955
Quick Facts
- NPI
- 1639512841
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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